导致小鼠雄性不育和存活非整倍体的常染色体易位。 - Suppr

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Autosomal translocations causing male sterility and viable aneuploidy in the mouse.

作者信息

Lyon M F, Meredith R

出版信息

Cytogenetics. 1966;5(5):335-54. doi: 10.1159/000129909.

DOI:10.1159/000129909

PMID:5958877

Abstract

摘要

相似文献

Autosomal translocations causing male sterility and viable aneuploidy in the mouse.导致小鼠雄性不育和存活非整倍体的常染色体易位。

Cytogenetics. 1966;5(5):335-54. doi: 10.1159/000129909.

The occurrence of chromosomal aberrations in pre-spermatocytic cells of irradiated male mice. 3. Sterility and semisterility in the offspring of male mice irradiated in the pre-meiotic and post-meiotic stages of spermatogenesis.

Can J Genet Cytol. 1967 Mar;9(1):163-254. doi: 10.1139/g67-020.

Translocations, the predominant cause of total sterility in sons of mice treated with mutagens.易位是用诱变剂处理过的小鼠雄性后代完全不育的主要原因。

Genetics. 1974 Jan;76(1):73-91. doi: 10.1093/genetics/76.1.73.

Meiotic chromosome rearrangements induced in mice by irradiation of spermatogonial stages.精原细胞阶段受辐射诱导小鼠减数分裂染色体重排。

Can J Genet Cytol. 1966 Sep;8(3):520-7. doi: 10.1139/g66-062.

[Analysis of chromosome aberrations on the basis of synaptonemal complexes in the offspring of mice irradiated with gamma-rays].

Genetika. 1986 Jul;22(7):1119-26.

[Reproductive functioning and higher nervous activity of mice with chromosome T6 trisomy].

Fiziol Zh SSSR Im I M Sechenova. 1973 May;59(5):704-12.

EFFECTS OF CHRONIC LOW-DOSE IRRADIATION FOR THREE SUCCESSIVE GENERATIONS ON THE BREEDING BEHAVIOUR OF MICE.连续三代慢性低剂量辐射对小鼠繁殖行为的影响

Int J Radiat Biol Relat Stud Phys Chem Med. 1964;8:523-31. doi: 10.1080/09553006414550661.

Reduced incidence of persistent chromosome aberrations in mice irradiated at low dose-rate.低剂量率照射小鼠后持续性染色体畸变发生率降低。

Res Dev Tech Rep. 1963 May 6:1-10.

Accumulation of chromosome damage under continuous low dose rate exposure.连续低剂量率照射下染色体损伤的累积

Radiology. 1967 Apr;88(4):767-74. doi: 10.1148/88.4.767.

Induction of translocations in mouse spermatogonia by X-ray doses divided into many small fractions.通过将X射线剂量分成许多小份来诱导小鼠精原细胞中的易位。

Mutat Res. 1970 Feb;9(2):219-23. doi: 10.1016/0027-5107(70)90060-6.

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Clinical outcomes in carriers of insertional translocation: a retrospective analysis of comprehensive chromosome screening results.插入性易位携带者的临床结局：综合染色体筛查结果的回顾性分析

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Unique case reports associated with ovarian failure: necessity of two intact x chromosomes.与卵巢功能衰竭相关的独特病例报告：两条完整X染色体的必要性。

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Segmental trisomy of mouse chromosome 17: introducing an alternative model of Down's syndrome.小鼠17号染色体节段性三体：引入唐氏综合征的另一种模型。

Comp Funct Genomics. 2003;4(6):647-52. doi: 10.1002/cfg.334.

Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes.17号染色体节段性三体：人类非整倍体综合征的小鼠模型

Proc Natl Acad Sci U S A. 2005 Mar 22;102(12):4500-5. doi: 10.1073/pnas.0500802102. Epub 2005 Mar 8.

Retardation of ovarian growth in male-sterile mice carrying an autosomal translocation.携带常染色体易位的雄性不育小鼠卵巢生长迟缓。

J Med Genet. 1981 Dec;18(6):414-7. doi: 10.1136/jmg.18.6.414.

A complex rearrangement involving three autosomes in a phenotypically normal male presenting with sterility.一名表现为不育的表型正常男性中涉及三条常染色体的复杂重排。

J Med Genet. 1982 Oct;19(5):375-7. doi: 10.1136/jmg.19.5.375.

XY pair associates with the synaptonemal complex of autosomal male-sterile translocations in pachytene spermatocytes of the mouse (Mus musculus).XY 配对与小鼠（小家鼠）粗线期精母细胞中常染色体雄性不育易位的联会复合体相关。

Chromosoma. 1981;82(1):41-53. doi: 10.1007/BF00285748.

Pachytene chromosomes in male and female mice heterozygous for the Is(7;1)40H insertion.

Chromosoma. 1984;90(3):163-9. doi: 10.1007/BF00292392.

The identification of the chromosome bearing linkage group XII in the mouse.小鼠中携带连锁群 XII 的染色体的鉴定。

Genetics. 1971 Oct;69(2):267-71. doi: 10.1093/genetics/69.2.267.

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